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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 399883Generated: October 26, 2026

Chlorambucil → Indole-3-Acetic Acid

https://huagongshe.com/reaction/399883

Reaction equation

Participants

RoleNameHCIDCharge
ReactantChlorambucilHCID 2708—
Reactant1H-Indole-3-propanoic acidHCID 3744—
ReactantIndole-3-Butyric AcidHCID 8617—
Reactant5-Methoxyindoleacetic acidHCID 18986—
ReactantFlavone-8-Acetic AcidHCID 55748—
ReactantBenzo-1,3-dioxole-5-acetic acidHCID 76115—
Reactant2-Methyl-1H-indole-3-acetic acidHCID 589107—
Reactant3,4-Methylenedioxycinnamic acidHCID 643181—
Reactant2-Indolylacetic acidHCID 4371752—
ProductIndole-3-Acetic AcidHCID 802—

Reaction Steps

2-indolylacetic acid; (N-methyl)-2- or -3-indolylacetic acid; 3-(3-indolyl)propionic acid; 3- or 2-indolylacrylic acid (also (N-methyl)); (2-methyl-3-indolyl)acetic acid, 3,4-(methylenedioxy)phenylacetic acid; 3,4-(methylenedioxy)cinnamic acid; indole-3-butyric acid; (5-methoxyindol-3-yl)acetic acid; naphthyl-1- or -2-acetic acid; flavone-8-acetic acid; 5,6-dimethylxanthone-4-acetic acid (L. L. Thomsen et al.: Cancer Chemother, Pharmacol. 31, 151ff. (1992) demonstrate that the corticoid 21-carboxylic esters prepared from this could also have an antitumorigenic effect, likewise the abovementioned chlorambucil).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05824670
Source datasetuspto-grants-1998_10
ORD IDord-f17162eee9fd4fa2a1cf4cb44ea995ed
Source noteuspto-grants-1998_10