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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1433780Generated: October 26, 2026

Bromomethylcyclopropane → (R)-tert-butoxycarbonylamino-[4-(2-tert-butoxy-ethoxy)-phenyl]-acetic acid

https://huagongshe.com/reaction/1433780

Reaction equation

Participants

RoleNameHCIDCharge
ReactantBromomethylcyclopropaneHCID 81503—
Reactant2-Chloro-4-iodoanilineHCID 282930—
Reactant(R)-tert-butoxycarbonylamino-{4-[2-(tetrahydropyran-2-yloxy)-ethoxy]-phenyl}-acetic acidHCID 68617730—
Reactant(R)-tert-butoxycarbonylamino-(4-cyclopropylmethoxy-phenyl)-acetic acidHCID 68618840—
Product(R)-tert-butoxycarbonylamino-[4-(2-tert-butoxy-ethoxy)-phenyl]-acetic acidHCID 66815165—

Reaction Steps

Prepared by the same method as described in example 3 except that 2-chloro-4-iodoaniline was used in place of 2-chloro-4-bromoaniline in step 1 and (R)-tert-butoxycarbonylamino-(4-cyclopropylmethoxy-phenyl)-acetic acid was used in place of (R)-tert-butoxycarbonylamino-[4-(2-tert-butoxy-ethoxy)-phenyl]-acetic acid in step 2. (R)-tert-butoxycarbonylamino-[4-(2-tert-butoxy-ethoxy)-phenyl]-acetic acid was prepared by a similar method as described for the preparation of (R)-tert-butoxycarbonylamino-{4-[2-(tetrahydro-pyran-2-yloxy)-ethoxy]-phenyl}-acetic acid in example 48 except that cyclopropylmethyl bromide was used in place of 2-(2-bromo-ethoxy)-tetrahydropyran.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07612212B2
Source datasetuspto-grants-2009_11
ORD IDord-a82a85bcf2a7400eafa7e8df296a6c09
Source noteuspto-grants-2009_11