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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 567435Generated: October 30, 2026

HCID 70220605, compound → HCID 54257512, compound

https://huagongshe.com/reaction/567435

Reaction equation

Participants

RoleNameHCIDCharge
ReactantHCID 70220605HCID 70220605—
ReactantHCID 70221359HCID 70221359—
ReactantHCID 86756292HCID 86756292—
ReactantHCID 86756294HCID 86756294—
ProductHCID 54257512HCID 54257512100%
ProductHCID 70217343HCID 70217343100%
ProductHCID 70219721HCID 70219721100%
ProductHCID 70220200HCID 70220200100%

Reaction Steps

The procedure of Example 6 was repeated, except that 17-cyclopropylmethyl-3,14β-dihydroxy-4,5α-epoxy-6β-(N-isopropylbenzylamino)morphinan dihydrochloride 191, 17-cyclopropylmethyl-3,14β-dihydroxy-4,5α-epoxy-6β-(N-isobutylbenzylamino)morphinan dihydrochloride 192, 17-cyclopropylmethyl-3,14β-dihydroxy-4,5α-epoxy-6β-(N-butylbenzylamino)morphinan dihydrochloride 193 and 17-cyclopropylmethyl-3,14β-dihydroxy-4,5α-epoxy-6β-(N-pentylbenzylamino)morphinan dihydrochloride 194 were used as the starting compound instead of 6β-(N-benzyl)methylamino-17-cyclopropylmethyl-4,5α-epoxy-3,14β-dihydroxymorphinan 8 hydrochloride, thereby preparing 17-cyclopropylmethyl-3,14β-dihydroxy-4,5α-epoxy-6β-isopropylaminomorphinan 195 (yield: 100%), 17-cyclopropylmethyl-3,14β-dihydroxy-4,5α-epoxy-6β-isobutylaminomorphinan 196 (yield: 100%), 17-cyclopropylmethyl-3,14β-dihydroxy-4,5α-epoxy-6β-butylaminomorphinan 197 (yield: 100%) and 17-cyclopropylmethyl-3,14β-dihydroxy-4,5α-epoxy-6β-pentylaminomorphinan 198 (yield: 100%).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06177438B1
Source datasetuspto-grants-2001_01
ORD IDord-ae54fea57e95419bb4bc04391945d01d
Source noteuspto-grants-2001_01