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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 17244Generated: October 29, 2026

Chloride → HCID 135772713, compound

https://huagongshe.com/reaction/17244

Reaction equation

Participants

RoleNameHCIDCharge
ReactantChlorideHCID 312—
Reactantethyl (Z)-5-{[(benzyloxy)carbonyl]amino}-3-tetrahydro-1H-1-pyrrolyl-2-pentenoateHCID 86596702—
ReactantHCID 135536110HCID 135536110—
ProductHCID 135772713HCID 135772713—

Reaction Steps

The title compound was prepared from 4-phenoxybenzohydroxyiminoyl chloride, prepared using the procedure described in Jones, Raymond C. F. et al, J. Med. Chem. 2003, 46, 87-96, and ethyl (Z)-5-{[(benzyloxy)carbonyl]amino}-3-tetrahydro-1H-1-pyrrolyl-2-pentenoate, prepared using the procedure described in Natale, Nicholas, R. et al, J. Chem. Soc. Perkins Trans. I, 1999, 765-776, using a manner similar to that described in Natale, Nicholas, R. et al, J. Chem. Soc. Perkins Trans. I, 1999, 765-776 for the preparation of 3-methyl-4,5-dihydroisoxazolo[4,5-c]pyridin-4-one. 1H NMR (DMSO-d6, 400 MHz) δ8.31 (d, 2H), 7.66 (d, 1H), 7.46 (t, 2H), 7.22 (t, 1H), 7.1-7.15 (m, 5H), 6.82 (d, 1H); Rt=3.03 min (Conditions a), MS m/e: 303 (M−H)−.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07737160B2
Source datasetuspto-grants-2010_06
ORD IDord-5daccee6f7804a778a610f894b45d86c
Source noteuspto-grants-2010_06